Canonical Allele Identifier: CA411817127
Gene: TSPO HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.43558945G>C (hg19) chr22:g.43162939G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162939G>C , CM000684.2:g.43162939G>C GRCh38
NC_000022.10:g.43558945G>C , CM000684.1:g.43558945G>C GRCh37
NC_000022.9:g.41888889G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337554.8:c.458G>C MANE Select ENSP00000338004.3:p.Cys153Ser
ENST00000329563.8:c.458G>C ENSP00000328973.4:p.Cys153Ser
ENST00000337554.7:c.458G>C ENSP00000338004.3:p.Cys153Ser
ENST00000396265.4:c.458G>C ENSP00000379563.4:p.Cys153Ser
ENST00000583777.5:c.146G>C ENSP00000463495.1:p.Cys49Ser
NM_000714.5:c.458G>C NP_000705.2:p.Cys153Ser
NM_001256530.1:c.458G>C NP_001243459.1:p.Cys153Ser
NM_001256531.1:c.458G>C NP_001243460.1:p.Cys153Ser
NR_046308.1:n.367G>C
NM_000714.6:c.458G>C MANE Select NP_000705.2:p.Cys153Ser
NR_046308.2:n.322G>C
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